ENST00000682617.1:c.2453G>A
|
ENSP00000507912.1:p.Arg818Gln
|
|
ENST00000683962.1:c.*2009G>A
|
ENSP00000506854.1:n.*2009G>A
|
|
ENST00000311895.8:c.2315G>A
MANE Select
|
ENSP00000310520.7:p.Arg772Gln
|
|
ENST00000311895.7:c.2315G>A
|
ENSP00000310520.7:p.Arg772Gln
|
|
ENST00000389138.7:n.1592G>A
|
|
|
ENST00000462862.1:c.628G>A
|
ENSP00000461322.1:n.628G>A
|
|
NM_005236.2:c.2315G>A , LRG_463t1:c.2315G>A
|
NP_005227.1:p.Arg772Gln
|
|
XM_011522424.1:c.2453G>A
|
XP_011520726.1:p.Arg818Gln
|
|
XM_011522425.1:c.1772G>A
|
XP_011520727.1:p.Arg591Gln
|
|
XM_011522426.1:c.1526G>A
|
XP_011520728.1:p.Arg509Gln
|
|
XM_011522427.1:c.965G>A
|
XP_011520729.1:p.Arg322Gln
|
|
XR_932805.1:n.2474G>A
|
|
|
XM_011522424.3:c.2453G>A
|
XP_011520726.1:p.Arg818Gln
|
|
XM_017023043.2:c.1526G>A
|
XP_016878532.1:p.Arg509Gln
|
|
NM_005236.3:c.2315G>A
MANE Select
|
NP_005227.1:p.Arg772Gln
|
|